D. Hunden

SYNTHESIS AND STRUCTURE-ACTIVITY RELATIONSHIPS OF BENZOPHENONES AS INHIBITORS OF CATHEPSIN D

D. R. Berry, S. Little, C. Whitesitt, 1996 .

Rapid parallel synthesis applied to the optimization of a series of potent nonpeptide neuropeptide Y-1 receptor antagonists

M. Siegel, P. Ornstein, M. Clay, 1999 .

LY320135, a novel cannabinoid CB1 receptor antagonist, unmasks coupling of the CB1 receptor to stimulation of cAMP accumulation.

K. Mackie, M. Glass, M. Brownstein, 1998, The Journal of pharmacology and experimental therapeutics.

Azetidinones as vasopressin V1a antagonists.

C. Ferris, M. Brownstein, M. Clay, 2007, Bioorganic & medicinal chemistry.

LY 320135 , a Novel Cannabinoid CB 1 Receptor Antagonist , Unmasks Coupling of the CB 1 Receptor to Stimulation of cAMP Accumulation 1

K. Mackie, M. Glass, M. Brownstein, 1997 .

Molecular modeling of γ-lactam analogues of β-lactam antibacterial agents: synthesis and biological evaluation of selected penem and carbapenem analoques

Donald B. Boyd, John E. Munroe, Jack B. Deeter, 1989 .

Orally absorbable cephalosporin antibiotics. 2. Structure-activity studies of bicyclic glycine derivatives of 7-aminodeacetoxycephalosporanic acid.

D. Hunden, J. Ott, F. T. Counter, 1985, Journal of medicinal chemistry.

The synthesis of the 14C and 2H‐isotopomers of (R)‐N‐[2‐(2′‐ethoxyphenoxy)‐ethyl]‐N‐2‐[3‐(4′‐methoxy‐3′‐sulfonamido)‐phenyl]‐propylamine hydrochloride, an α1‐adrenoreceptor antagonist

W. J. Wheeler, D. Hunden, K. K. Schmiegel, 1989 .

Molecular Modeling of γ-Lactam Analogues of β-Lactam Antibacterial Agents: Synthesis and Biological Evaluation of Selected Penem and Carbapenem Analogues.

J. M. Morin, D. B. Boyd, J. Deeter, 1989 .